de Leon M, Wang Y, Jones L, Perez-Reyes E, Wei X, Soong T W, Snutch T P, Yue D T
Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Science. 1995 Dec 1;270(5241):1502-6. doi: 10.1126/science.270.5241.1502.
Intracellular calcium (Ca2+) inhibits the opening of L-type (alpha 1C) Ca2+ channels, providing physiological control of Ca2+ entry into a wide variety of cells. A structural determinant of this Ca(2+)-sensitive inactivation was revealed by chimeric Ca2+ channels derived from parental alpha 1C and alpha 1E channels, the latter of which is a neuronal channel lacking Ca2+ inactivation. A consensus Ca(2+)-binding motif (an EF hand), located on the alpha 1C subunit, was required for Ca2+ inactivation. Donation of the alpha 1C EF-hand region to the alpha 1E channel conferred the Ca(2+)-inactivating phenotype. These results strongly suggest that Ca2+ binding to the alpha 1C subunit initiates Ca2+ inactivation.
细胞内钙(Ca2+)抑制L型(α1C)Ca2+通道的开放,从而对多种细胞中Ca2+的内流进行生理调控。通过源自亲代α1C和α1E通道的嵌合Ca2+通道,揭示了这种Ca2+敏感失活的一个结构决定因素,其中α1E通道是一种缺乏Ca2+失活的神经元通道。位于α1C亚基上的一个共有Ca2+结合基序(一个EF手)是Ca2+失活所必需的。将α1C的EF手区域赋予α1E通道可使其具有Ca2+失活表型。这些结果有力地表明,Ca2+与α1C亚基的结合启动了Ca2+失活。